2-Butenoic acid, phenylmethyl ester

Details

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Internal ID 4e1af97d-6d07-4fe5-ad7f-0d5cb75fbbd9
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzyloxycarbonyls
IUPAC Name benzyl but-2-enoate
SMILES (Canonical) CC=CC(=O)OCC1=CC=CC=C1
SMILES (Isomeric) CC=CC(=O)OCC1=CC=CC=C1
InChI InChI=1S/C11H12O2/c1-2-6-11(12)13-9-10-7-4-3-5-8-10/h2-8H,9H2,1H3
InChI Key NCPTYZLUYHXITE-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H12O2
Molecular Weight 176.21 g/mol
Exact Mass 176.083729621 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.31
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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65416-24-2
Benzyl 2-butenoate
Benzyl but-2-enoate
DTXSID0070318
FT-0622839
W13679

2D Structure

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2D Structure of 2-Butenoic acid, phenylmethyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8755 87.55%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6691 66.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9150 91.50%
OATP1B3 inhibitior + 0.9667 96.67%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7441 74.41%
P-glycoprotein inhibitior - 0.9873 98.73%
P-glycoprotein substrate - 0.9849 98.49%
CYP3A4 substrate - 0.6310 63.10%
CYP2C9 substrate + 0.5928 59.28%
CYP2D6 substrate - 0.9017 90.17%
CYP3A4 inhibition - 0.9691 96.91%
CYP2C9 inhibition - 0.9032 90.32%
CYP2C19 inhibition - 0.8395 83.95%
CYP2D6 inhibition - 0.9539 95.39%
CYP1A2 inhibition + 0.6829 68.29%
CYP2C8 inhibition - 0.7058 70.58%
CYP inhibitory promiscuity - 0.6120 61.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5384 53.84%
Carcinogenicity (trinary) Non-required 0.6755 67.55%
Eye corrosion + 0.8179 81.79%
Eye irritation + 0.9799 97.99%
Skin irritation + 0.8783 87.83%
Skin corrosion - 0.8245 82.45%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5764 57.64%
Micronuclear - 0.8941 89.41%
Hepatotoxicity - 0.6448 64.48%
skin sensitisation + 0.9006 90.06%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity - 0.6433 64.33%
Acute Oral Toxicity (c) III 0.9418 94.18%
Estrogen receptor binding - 0.7663 76.63%
Androgen receptor binding - 0.5829 58.29%
Thyroid receptor binding - 0.8244 82.44%
Glucocorticoid receptor binding - 0.7547 75.47%
Aromatase binding - 0.5294 52.94%
PPAR gamma - 0.7898 78.98%
Honey bee toxicity - 0.9402 94.02%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.5955 59.55%
Fish aquatic toxicity + 0.9540 95.40%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.85% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.74% 86.33%
CHEMBL2581 P07339 Cathepsin D 92.00% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.14% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.00% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 90.56% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 87.53% 94.73%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.53% 94.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.84% 95.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Carica papaya

Cross-Links

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PubChem 97885
LOTUS LTS0242589
wikiData Q81997573